Evidence map›Paper›PMID 42734136›Full record

ArticleActa orthopaedica2026

Should we remove flexible intramedullary nails after diaphyseal forearm pediatric fracture? A cohort study of 288 patients.

Maria Tirta, Amalie Eikrem-Holsæter, Eline Borg Holt, Richard Olsson, Rune Bruhn Jakobsen, Per-Henrik Randsborg

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Article in Acta orthopaedica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Maria TirtaDepartment of Orthopedic Surgery, Akershus University Hospital, Oslo, Norway; Interdisciplinary Orthopaedics, Aalborg University Hospital, Aalborg, Denmark. m.tirta@rn.dk.
Amalie Eikrem-HolsæterFaculty of Medicine, University of Oslo, Oslo, Norway.
Eline Borg HoltFaculty of Medicine, University of Oslo, Oslo, Norway.
Richard OlssonDepartment of Orthopedic Surgery, Akershus University Hospital, Oslo, Norway.
Rune Bruhn JakobsenDepartment of Orthopedic Surgery, Akershus University Hospital, Oslo, Norway; Faculty of Medicine, University of Oslo, Oslo, Norway.
Per-Henrik RandsborgDepartment of Orthopedic Surgery, Akershus University Hospital, Oslo, Norway; Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0002-7674-1572

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeRoutine removal of elastic stable intramedullary nails (ESIN) after pediatric diaphyseal forearm fractures remains common practice despite limited supporting evidence. We aimed to evaluate refracture risk following ESIN retention compared with implant removal and assessed complications and healthcare resource use.

methodsIn this retrospective cohort study, patients treated with ESIN for diaphyseal forearm fractures at a single center were included. Following a policy change, routine implant removal was discontinued in favor of retaining implants unless symptomatic. Patients were grouped into removal and non-removal. The primary outcome was refracture, analyzed using Cox regression, and early refractures (< 12 months), using logistic regression. Secondary outcomes included complications and healthcare resource utilization (outpatient visits, radiographic examinations during follow-up).

results288 patients were included, of whom 136 underwent implant removal and 152 retained their implants. Among patients with implant retention, 9/152 (5.9%) subsequently required removal, most commonly due to implant-related irritation. Refracture occurred in 13/136 (9.6%) after implant removal and 8/152 (5.3%) after implant retention (absolute risk difference 4.3 percentage points, 95% confidence interval [CI] -1.8 to 10.4; HR 1.4, CI 0.5-3.4). Early refracture occurred in 8/136 (5.9%) patients after implant removal and 5/152 (3.3%) after implant retention (absolute risk difference 2.6 percentage points, CI -2.3 to 7.5; OR 1.8, CI 0.6-6.2), including 3 cases within 6 months after removal. Complications occurred in 11/136 (8.1%) patients after implant removal. Infection occurred in 5/136 (3.7%) after implant removal vs 4/288 (1.4%) after the initial surgery (risk difference 2.3 percentage points, CI -1.2 to 5.7).

conclusionESIN retention was well tolerated and associated with reduced healthcare utilization. No clear difference in refracture risk was observed between groups, although the study was not powered to detect moderate differences in risk.

Indexed as

Bone NailsDevice RemovalFracture Fixation, IntramedullaryRadius FracturesUlna FracturesAdolescentChildChild, PreschoolCohort StudiesDiaphysesFemaleHardware RemovalHumansMaleRecurrenceRetrospective Studies

Identifiers

PMID42734136
PMCPMC13572937

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.